US20150112102A1 - System and method for removal of heavy metal ions from a rich hydrate inhibitor stream - Google Patents
System and method for removal of heavy metal ions from a rich hydrate inhibitor stream Download PDFInfo
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- US20150112102A1 US20150112102A1 US14/404,519 US201314404519A US2015112102A1 US 20150112102 A1 US20150112102 A1 US 20150112102A1 US 201314404519 A US201314404519 A US 201314404519A US 2015112102 A1 US2015112102 A1 US 2015112102A1
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- Prior art keywords
- hydrate inhibitor
- heavy metal
- stream
- outlet
- rich
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- Granted
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- 239000003112 inhibitor Substances 0.000 title claims abstract description 105
- 229910001385 heavy metal Inorganic materials 0.000 title claims abstract description 69
- 238000000034 method Methods 0.000 title claims abstract description 50
- 150000002500 ions Chemical class 0.000 title claims abstract description 15
- 150000003839 salts Chemical class 0.000 claims abstract description 38
- 239000012530 fluid Substances 0.000 claims abstract description 21
- 239000002245 particle Substances 0.000 claims abstract description 16
- 239000002002 slurry Substances 0.000 claims abstract description 15
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 14
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 14
- 239000000376 reactant Substances 0.000 claims abstract description 13
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 9
- 238000000926 separation method Methods 0.000 claims description 26
- 238000004891 communication Methods 0.000 claims description 12
- 238000001556 precipitation Methods 0.000 claims description 12
- -1 cation salts Chemical class 0.000 claims description 11
- 229910052753 mercury Inorganic materials 0.000 claims description 10
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 230000001105 regulatory effect Effects 0.000 claims description 6
- 150000004763 sulfides Chemical group 0.000 claims description 6
- VDQVEACBQKUUSU-UHFFFAOYSA-M disodium;sulfanide Chemical group [Na+].[Na+].[SH-] VDQVEACBQKUUSU-UHFFFAOYSA-M 0.000 claims description 5
- 229910052979 sodium sulfide Inorganic materials 0.000 claims description 5
- 238000011144 upstream manufacturing Methods 0.000 claims description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 3
- 229910052785 arsenic Inorganic materials 0.000 claims description 3
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 3
- 229910052793 cadmium Inorganic materials 0.000 claims description 3
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 239000011651 chromium Substances 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 239000011133 lead Substances 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 239000011572 manganese Substances 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 21
- 230000008929 regeneration Effects 0.000 description 11
- 238000011069 regeneration method Methods 0.000 description 11
- 150000001768 cations Chemical class 0.000 description 9
- 239000012071 phase Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 229910052788 barium Inorganic materials 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229910052791 calcium Inorganic materials 0.000 description 4
- 238000005755 formation reaction Methods 0.000 description 4
- 231100001261 hazardous Toxicity 0.000 description 4
- 239000002920 hazardous waste Substances 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 229910052712 strontium Inorganic materials 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 238000011143 downstream manufacturing Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000008398 formation water Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 150000002730 mercury Chemical class 0.000 description 2
- 239000002923 metal particle Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000002203 pretreatment Methods 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 235000021463 dry cake Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000011833 salt mixture Substances 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D21/00—Separation of suspended solid particles from liquids by sedimentation
- B01D21/26—Separation of sediment aided by centrifugal force or centripetal force
- B01D21/262—Separation of sediment aided by centrifugal force or centripetal force by using a centrifuge
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/88—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J14/00—Chemical processes in general for reacting liquids with liquids; Apparatus specially adapted therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J4/00—Feed or outlet devices; Feed or outlet control devices
- B01J4/001—Feed or outlet devices as such, e.g. feeding tubes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B04—CENTRIFUGAL APPARATUS OR MACHINES FOR CARRYING-OUT PHYSICAL OR CHEMICAL PROCESSES
- B04B—CENTRIFUGES
- B04B1/00—Centrifuges with rotary bowls provided with solid jackets for separating predominantly liquid mixtures with or without solid particles
- B04B1/04—Centrifuges with rotary bowls provided with solid jackets for separating predominantly liquid mixtures with or without solid particles with inserted separating walls
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B04—CENTRIFUGAL APPARATUS OR MACHINES FOR CARRYING-OUT PHYSICAL OR CHEMICAL PROCESSES
- B04B—CENTRIFUGES
- B04B7/00—Elements of centrifuges
- B04B7/08—Rotary bowls
- B04B7/12—Inserts, e.g. armouring plates
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/52—Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B21/00—Methods or apparatus for flushing boreholes, e.g. by use of exhaust air from motor
- E21B21/06—Arrangements for treating drilling fluids outside the borehole
- E21B21/068—Arrangements for treating drilling fluids outside the borehole using chemical treatment
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2208/00—Aspects relating to compositions of drilling or well treatment fluids
- C09K2208/22—Hydrates inhibition by using well treatment fluids containing inhibitors of hydrate formers
Definitions
- the present invention relates to a method for removal of heavy metal ions from a rich hydrate inhibitor stream and a heavy metal ions removal system. Especially the present invention relates to a method for controlled precipitation of heavy metal ion salts so that they are obtained as a separate fraction.
- hydrate inhibitors are added to the well stream prior to transportation.
- One often applied hydrate inhibitor is mono-ethylene glycol (MEG); other applicable hydrate inhibitors include glycol compounds with other substituents, as well as kinetic hydrate inhibitors or a combination thereof.
- MEG mono-ethylene glycol
- kinetic refers to the effect of the inhibitor lowering the reaction rate of the hydrate forming reactions.
- Hydrate inhibitors such as MEG are valuable chemicals and the recycling thereof provides reduced costs.
- a number of different steps and methods for separating MEG for reuse are known in the art.
- An obstacle for the regeneration process is degradation of the inhibitor at high temperatures which limits the possibility to use heating to obtain separation.
- the recovered well stream will comprise not only the desired hydrocarbons, hydrate inhibitor, employed chemicals such as pH stabilizer and formation water, but also different ions dissolved from the formation.
- Traditional hydrate inhibitor recovery and reclamation systems have been developed to remove ions in the form of precipitated salts from the recovered hydrate inhibitor to control the salt concentration and allow for continued reuse of the hydrate inhibitor.
- the most common precipitated salts are chlorides, carbonates or hydroxides of Na, K, Ca, Mg, Fe or Ba. These precipitated salts are not considered especially harmful and the safe handling thereof can be relatively easily secured. Recently, however there has been discovered a number of formations which comprise heavy metals including mercury in such a form that the mercury ions are included in the well stream.
- the mercury ions will follow the hydrate inhibitor into the reclamation system and be precipitated in the form of mercury salts together with the other salts present in the rich hydrate inhibitor stream.
- the separated salts will be a mixture comprising mercury salts and the total salt mixture must be treated as hazardous waste.
- the amounts of salts removed per day is in the range 1 to 20 tonnes/day.
- the main part of the salts is NaCl. If heavy metal salts are introduced in this mixture then the total salts produced become hazardous waste that requires special treatment. This is very demanding especially on offshore installations.
- the objective of the present invention is to provide a method and a system applicable to reduce the amount of hazardous waste produced from regeneration of hydrate inhibitor streams comprising heavy metals.
- a further goal is to minimize the process part and the process equipment that is handling process streams comprising hazardous heavy metals or metal ions.
- Another intension is to provide a method and system which can be retrofitted on existing systems or included in the new process.
- the present invention provides a method for removal of heavy metal ions from a rich hydrate inhibitor stream, wherein the method comprises
- the recovered rich hydrate inhibitor stream is substantially heavy metal free.
- the recovered rich hydrate inhibitor stream can be further processed according to well known processes for regeneration of rich hydrate inhibitor to obtain lean hydrate inhibitor applicable for reuse.
- the recovered rich hydrate inhibitor stream comprises in addition to the hydrate inhibitor water and non-heavy metal salts, and depending on the separation efficiency of step b) the recovered rich inhibitor may or may not contain a hydrocarbon rest.
- the separation in step b) is performed in a disc stack centrifuge.
- the method comprises regulating the pH of the rich hydrate inhibitor stream to between 6 and 8.
- the method comprises regulating the temperature of the rich hydrate inhibitor stream to below 30° C.
- the heavy metal is selected from the group mercury, cadmium, lead, chromium, cobalt, arsenic, nickel, manganese and copper, preferably mercury.
- the method comprises combining the remaining hydrate inhibitor with the recovered rich hydrate inhibitor stream.
- the selectivity of the reactant and the control of pH and temperature other divalent cations such as Fe, Ca, Ba, Sr, Mg are dissolved in the hydrate inhibitor through out the heavy metal removal.
- the method may accordingly further comprise downstream precipitation and removal of divalent cation salts from the recovered rich hydrate inhibitor stream.
- the selective heavy metal reactant is a sulphide, preferably Na 2 S.
- the method further comprises adding a flocculent to the rich hydrate inhibitor stream.
- the hydrate inhibitor is a glycol based inhibitor, especially the hydrate inhibitor is mono-ethylene-glycol (MEG).
- MEG mono-ethylene-glycol
- the present invention further provides a rich hydrate inhibitor heavy metal ions removal system comprising a reaction tank with a rich hydrate inhibitor inlet, at least one heavy metal ions reactant inlet, and a reacted rich hydrate inhibitor outlet in fluid communication with a three phase disc stack centrifuge comprising a hydrocarbon outlet, a recovered hydrate inhibitor outlet and a slurry outlet.
- system further comprises a separation unit with an inlet in fluid communication with the slurry outlet, a heavy metal salt outlet and a remaining hydrate inhibitor outlet.
- system comprises a fluid line with an inlet in fluid communication with the remaining hydrate inhibitor outlet and an outlet in fluid communication with the recovered hydrate inhibitor outlet and a pretreatment system.
- the removal system comprises a return loop for regulated returning of the remaining hydrate inhibitor upstream the separation unit.
- the return loop allows for returning of remaining hydrate inhibitor from the remaining inhibitor outlet to the separation unit if the separation achieved was not effective enough.
- the removal system may comprise a return line with an inlet in fluid communication with the remaining hydrate inhibitor outlet and an outlet in fluid communication with the reacted hydrate inhibitor outlet and the three phase disc stack centrifuge.
- heavy metals refers to environmental toxic heavy metals.
- the term covers for instance the elements mercury, cadmium, lead, chromium, cobalt, arsenic, nickel, manganese and copper.
- heavy metal ions refer to ions of the above defined heavy metals.
- hydrate inhibitor refers to hydrate inhibitors such as glycol based inhibitors like mono-ethylene-glycol (MEG), di-ethylene-glycol (DEG) and tri-ethylene-glycol (TEG), tetra-ethylene-glycol (TREG) or combinations thereof.
- glycol based inhibitors like mono-ethylene-glycol (MEG), di-ethylene-glycol (DEG) and tri-ethylene-glycol (TEG), tetra-ethylene-glycol (TREG) or combinations thereof.
- TEG mono-ethylene-glycol
- TEG tri-ethylene-glycol
- TEG tri-ethylene-glycol
- TMG tetra-ethylene-glycol
- kinetic hydrate inhibitors named so after by their ability to slow down the hydrate forming reactions and well known in the art or any combination of glycol based inhibitor(s) and kinetic inhibitors.
- rich hydrate inhibitor refers to a hydrate inhibitor stream which has not yet been subject to a substantial regeneration and/or reclamation process and which therefore comprises in addition to the hydrate inhibitor significant amounts of water, hydrocarbons, and dissolved salts in addition to dissolved heavy metal salts.
- the salts in addition to the heavy metal salts include monovalent and divalent cations, such as cations of alkali metals and alkali earth metals, Fe-ions etc. and anions such as halogen (Cl, Br, F, I), carbonate, hydroxide, etc.
- the hydrate inhibitor is referred to as lean hydrate inhibitor or alternatively as partly lean hydrate inhibitor if further regeneration steps are envisaged or the system does not require that substantially all salts are removed prior to reuse.
- the present invention provides not only a method and system for removal of heavy metals from a hydrate inhibitor stream but more specifically a system for removal of heavy metals from a rich hydrate inhibitor stream, and providing a substantially heavy metal free rich hydrate inhibitor stream that can be regenerated into a lean hydrate inhibitor stream by conventional methods.
- the heavy metal salts are obtained as separate fraction whereas all other salts can be separated via conventionally systems thereby obtaining a heavy metal free salt waste stream. Accordingly the present invention provides a selective heavy metal ion removal method and system.
- the heavy metals are separated in an upstream system providing the benefit of keeping the traditional pretreatment system, regeneration and reclamation system heavy metal free.
- the heavy metals are separated in a small fraction significantly smaller than the salt fractions obtained from pre-treatment and reclamation system.
- the present invention introduces a three phase disc stack centrifuge separator, where hydrocarbon separation significantly increases the efficiency of the downstream processes, including pre-treatment, regeneration and reclamation. This will especially improve the performance of the gravity separator and centrifuges employed for separating divalent cation salts during pretreatment. Hydrocarbon content in the produced water is also reduced considerably, increasing the quality of the water to be disposed or further used in the process. This also minimises the complexity of the possible produced water treatment facility.
- the three phase disc stack centrifuge can be operated at optimal flow rates, according to the following equations:
- the reactant is a sulphide source such as Na 2 S.
- a sulphide source such as Na 2 S.
- adding a sulphide may provide a selective reaction of heavy metal to precipitate as sulphide, which can be applied to solve the goals of the present invention.
- FIG. 1 illustrates schematically a first embodiment of the present invention
- FIG. 2 illustrates schematically a second embodiment of the present invention
- FIG. 3 illustrates schematically a third embodiment of the present invention
- FIG. 4 shows a block diagram of an embodiment of the present invention.
- FIG. 1 shows a first embodiment of the present invention.
- the flocculent is introduced to increase particle size of the precipitate and thereby improving the particle separation.
- the selectivity of the reactant towards the heavy metal may be influenced by the temperature and the pH of the mixture and optionally coolers or heaters may be installed upstream the on conduit 1 .
- the residence time in the tank 10 is adapted to secure precipitation of the heavy metal.
- the reacted rich hydrate inhibitor leaves the tank via line 13 and pump 14 , the rich hydrate inhibitor is fed to a three-phase disk stack centrifuge 20 through line 15 .
- This three phase separator provides not only separation of the precipitated heavy metal salts from the hydrate inhibitor but also separation of remaining hydrocarbons.
- the hydrocarbons are removed through line 21 , the heavy metal free rich hydrate inhibitor through line 19 and the slurry containing the heavy metal particles through line 23 which feds the slurry to a second separation system 24 providing solid liquid separation.
- the liquid phase comprising particle free rich hydrate inhibitor is via line 29 combined with the main rich hydrate inhibitor stream 19 .
- the obtained concentrated heavy metal salt particles 27 will be handled further as hazardous waste.
- the combined rich hydrate inhibitor streams now enter what can be considered a traditional pretreatment system consisting of an initial tank 32 for precipitation of salts of divalent cations.
- the alkalinity in the tank 32 is controlled by addition of base through line 31 .
- bases include: Na 2 CO 3 , K 2 CO 3 , KOH, NaOH.
- An appropriate resident time to secure precipitation of the divalent cation salts is obtained through the tank 32 .
- the rich hydrate inhibitor is transferred via line 33 , pump 34 and line 35 to a second centrifuge 36 , preferably a disk stack centrifuge. Due to the earlier removal of remaining hydrocarbons the centrifuge 36 or gravity separator (not shown) will show improved performance.
- Stream 39 contains the separated divalent cation salts, whereas stream 37 contains partly rich hydrate inhibitor which is being fed to a traditional regeneration and reclamation system 40 providing conventional full stream or slipstream reclamation.
- the particles in stream 39 are non hazardous and neither are the monovalent cation salts that are removed from the hydrate inhibitor during reclamation.
- FIG. 2 illustrates another embodiment of the present invention wherein an embodiment of the particle separation system is described in further detail.
- the slurry stream 23 enters a buffer tank 22 from where it is being fed to a solid-liquid separation unit 26 .
- Solid-liquid separation unit 26 can be but is not limited to filter, basket centrifuge etc.
- the unit 26 may not provide acceptable separation and the liquid phase 28 is then return via valve 52 and line 53 to the buffer tank 22 .
- the quality of the separation is monitored by a sensor 50 . When the stream quality is increased and the valve 51 can be opened and the valve 52 closed. Stream 27 will be nearly dry cake of precipitated heavy metal, which can be disposed off safely.
- FIG. 2 Also illustrated on FIG. 2 is the optional installation of a second sensor or sampling unit 56 for measuring the efficiency of the heavy metal removal to avoid heavy metals from entering the pretreatment system.
- FIG. 3 illustrates an alternative embodiment of the present invention. Equal units are given equal reference signs. The difference compared to FIGS. 1 and 2 is that the liquid stream from the separation system leaving through valve 51 is passed as stream 30 back into the line 15 . This system provides the further advantage that in case that heavy metal particles are allowed to pass the filter they will be passed back to the three phase separator 20 and be separated of again. In this embodiment the valve 52 and the line 53 may be obsolete.
- FIG. 4 illustrates an embodiment of the present invention as a block diagram.
- the hydrate inhibitor is mono ethylene glycol (MEG).
- a rich MEG feed is fed to a heavy metal precipitation tank to which a precipitant source/reactant e.g. Na 2 S and flocculent to increase the size and separation of the particles is also fed.
- the reacted mixture is passed on to a disc stack centrifuge providing separation into three streams, a hydrocarbon/condensate stream, a recovered rich MEG stream and a Heavy metal sludge stream.
- the heavy metal sludge stream is separated in a solid-liquid separation system providing nearly dry heavy metal precipitate. The solid-liquid separation reduces the rest stream comprising the hazardous mercury to a minimum.
- the recovered rich MEG enters the pretreatment vessel wherein the alkalinity is controlled to provide for precipitation of salts of divalent cations.
- the salts are removed in a disk stack centrifuge or a gravity separator providing a divalent cation free rich MEG to regeneration and reclamation and a slurry comprising salts of divalent cations. This slurry will not contain hazardous mercury and therefore need not be treated accordingly.
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- General Life Sciences & Earth Sciences (AREA)
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- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
Abstract
Description
- The present invention relates to a method for removal of heavy metal ions from a rich hydrate inhibitor stream and a heavy metal ions removal system. Especially the present invention relates to a method for controlled precipitation of heavy metal ion salts so that they are obtained as a separate fraction.
- It is well known that well streams containing a mixture of fluids such as crude oil, condensate, formation water and gas during transportation may react and form solid hydrates resulting in i.e. blocked pipelines. To avoid and or limit the formation of these, hydrate inhibitors are added to the well stream prior to transportation. One often applied hydrate inhibitor is mono-ethylene glycol (MEG); other applicable hydrate inhibitors include glycol compounds with other substituents, as well as kinetic hydrate inhibitors or a combination thereof. The term kinetic refers to the effect of the inhibitor lowering the reaction rate of the hydrate forming reactions.
- Hydrate inhibitors such as MEG are valuable chemicals and the recycling thereof provides reduced costs. A number of different steps and methods for separating MEG for reuse are known in the art. An obstacle for the regeneration process is degradation of the inhibitor at high temperatures which limits the possibility to use heating to obtain separation.
- The recovered well stream will comprise not only the desired hydrocarbons, hydrate inhibitor, employed chemicals such as pH stabilizer and formation water, but also different ions dissolved from the formation. Traditional hydrate inhibitor recovery and reclamation systems have been developed to remove ions in the form of precipitated salts from the recovered hydrate inhibitor to control the salt concentration and allow for continued reuse of the hydrate inhibitor. The most common precipitated salts are chlorides, carbonates or hydroxides of Na, K, Ca, Mg, Fe or Ba. These precipitated salts are not considered especially harmful and the safe handling thereof can be relatively easily secured. Recently, however there has been discovered a number of formations which comprise heavy metals including mercury in such a form that the mercury ions are included in the well stream. In a traditional system the mercury ions will follow the hydrate inhibitor into the reclamation system and be precipitated in the form of mercury salts together with the other salts present in the rich hydrate inhibitor stream. However the separated salts will be a mixture comprising mercury salts and the total salt mixture must be treated as hazardous waste. In a standard traditional MEG reclamation system the amounts of salts removed per day is in the range 1 to 20 tonnes/day. The main part of the salts is NaCl. If heavy metal salts are introduced in this mixture then the total salts produced become hazardous waste that requires special treatment. This is very demanding especially on offshore installations.
- Different technical solutions have been developed to extract inhibitor and handle the inorganic salt problem. Examples of these techniques are disclosed in U.S. Pat. No. 6,340,373 and US2005/0072663 and US2010/019023.
- The objective of the present invention is to provide a method and a system applicable to reduce the amount of hazardous waste produced from regeneration of hydrate inhibitor streams comprising heavy metals.
- A further goal is to minimize the process part and the process equipment that is handling process streams comprising hazardous heavy metals or metal ions.
- It is also a goal to provide a process with limited negative or even positive influence on the efficiency of the downstream processes.
- Another intension is to provide a method and system which can be retrofitted on existing systems or included in the new process.
- The present invention provides a method for removal of heavy metal ions from a rich hydrate inhibitor stream, wherein the method comprises
-
- a) adding a selective heavy metal reactant to the rich hydrate inhibitor stream, forming a fluid stream comprising heavy metal salt particles,
- b) separating the obtained fluid stream in three streams a hydrocarbon stream, a recovered rich hydrate inhibitor stream, and a slurry comprising the heavy metal salt particles,
- c) separating remaining hydrate inhibitor from the slurry thereby obtaining a concentrated rest comprising the heavy metal salt particles.
- The recovered rich hydrate inhibitor stream is substantially heavy metal free. The recovered rich hydrate inhibitor stream can be further processed according to well known processes for regeneration of rich hydrate inhibitor to obtain lean hydrate inhibitor applicable for reuse. The recovered rich hydrate inhibitor stream comprises in addition to the hydrate inhibitor water and non-heavy metal salts, and depending on the separation efficiency of step b) the recovered rich inhibitor may or may not contain a hydrocarbon rest.
- In one aspect of the method according to the present invention the separation in step b) is performed in a disc stack centrifuge.
- In another aspect of the present invention the method comprises regulating the pH of the rich hydrate inhibitor stream to between 6 and 8.
- In yet another aspect the method comprises regulating the temperature of the rich hydrate inhibitor stream to below 30° C.
- The regulation of the pH close to neutral and having low temperature provides favourable condition for heavy metal precipitation at the same time limiting possibly avoiding precipitation of other divalent cations such as Fe, Ca, Ba, Sr, Mg.
- In a further aspect of the method according to the present invention the heavy metal is selected from the group mercury, cadmium, lead, chromium, cobalt, arsenic, nickel, manganese and copper, preferably mercury.
- In yet another aspect the method comprises combining the remaining hydrate inhibitor with the recovered rich hydrate inhibitor stream.
- In a further aspect of the method the selectivity of the reactant and the control of pH and temperature other divalent cations such as Fe, Ca, Ba, Sr, Mg are dissolved in the hydrate inhibitor through out the heavy metal removal. The method may accordingly further comprise downstream precipitation and removal of divalent cation salts from the recovered rich hydrate inhibitor stream.
- In a specific aspect of the present invention the selective heavy metal reactant is a sulphide, preferably Na2S.
- In another aspect of the invention the method further comprises adding a flocculent to the rich hydrate inhibitor stream.
- Further in one aspect of the invention the hydrate inhibitor is a glycol based inhibitor, especially the hydrate inhibitor is mono-ethylene-glycol (MEG).
- The present invention further provides a rich hydrate inhibitor heavy metal ions removal system comprising a reaction tank with a rich hydrate inhibitor inlet, at least one heavy metal ions reactant inlet, and a reacted rich hydrate inhibitor outlet in fluid communication with a three phase disc stack centrifuge comprising a hydrocarbon outlet, a recovered hydrate inhibitor outlet and a slurry outlet.
- In one aspect of the removal system according to the invention the system further comprises a separation unit with an inlet in fluid communication with the slurry outlet, a heavy metal salt outlet and a remaining hydrate inhibitor outlet.
- In another aspect the system comprises a fluid line with an inlet in fluid communication with the remaining hydrate inhibitor outlet and an outlet in fluid communication with the recovered hydrate inhibitor outlet and a pretreatment system.
- In yet another embodiment the removal system comprises a return loop for regulated returning of the remaining hydrate inhibitor upstream the separation unit. The return loop allows for returning of remaining hydrate inhibitor from the remaining inhibitor outlet to the separation unit if the separation achieved was not effective enough.
- Further the removal system may comprise a return line with an inlet in fluid communication with the remaining hydrate inhibitor outlet and an outlet in fluid communication with the reacted hydrate inhibitor outlet and the three phase disc stack centrifuge.
- The term “heavy metals” as used here refers to environmental toxic heavy metals. The term covers for instance the elements mercury, cadmium, lead, chromium, cobalt, arsenic, nickel, manganese and copper.
- The term “heavy metal ions” refer to ions of the above defined heavy metals.
- The term “hydrate inhibitor” as employed here refers to hydrate inhibitors such as glycol based inhibitors like mono-ethylene-glycol (MEG), di-ethylene-glycol (DEG) and tri-ethylene-glycol (TEG), tetra-ethylene-glycol (TREG) or combinations thereof. The term also refers to kinetic hydrate inhibitors, named so after by their ability to slow down the hydrate forming reactions and well known in the art or any combination of glycol based inhibitor(s) and kinetic inhibitors.
- The term “rich hydrate inhibitor” as used herein refers to a hydrate inhibitor stream which has not yet been subject to a substantial regeneration and/or reclamation process and which therefore comprises in addition to the hydrate inhibitor significant amounts of water, hydrocarbons, and dissolved salts in addition to dissolved heavy metal salts. The salts in addition to the heavy metal salts include monovalent and divalent cations, such as cations of alkali metals and alkali earth metals, Fe-ions etc. and anions such as halogen (Cl, Br, F, I), carbonate, hydroxide, etc. After a regeneration and/or reclamation process the hydrate inhibitor is referred to as lean hydrate inhibitor or alternatively as partly lean hydrate inhibitor if further regeneration steps are envisaged or the system does not require that substantially all salts are removed prior to reuse.
- The present invention provides not only a method and system for removal of heavy metals from a hydrate inhibitor stream but more specifically a system for removal of heavy metals from a rich hydrate inhibitor stream, and providing a substantially heavy metal free rich hydrate inhibitor stream that can be regenerated into a lean hydrate inhibitor stream by conventional methods. The heavy metal salts are obtained as separate fraction whereas all other salts can be separated via conventionally systems thereby obtaining a heavy metal free salt waste stream. Accordingly the present invention provides a selective heavy metal ion removal method and system.
- According to the present invention the heavy metals are separated in an upstream system providing the benefit of keeping the traditional pretreatment system, regeneration and reclamation system heavy metal free. The heavy metals are separated in a small fraction significantly smaller than the salt fractions obtained from pre-treatment and reclamation system.
- The present invention introduces a three phase disc stack centrifuge separator, where hydrocarbon separation significantly increases the efficiency of the downstream processes, including pre-treatment, regeneration and reclamation. This will especially improve the performance of the gravity separator and centrifuges employed for separating divalent cation salts during pretreatment. Hydrocarbon content in the produced water is also reduced considerably, increasing the quality of the water to be disposed or further used in the process. This also minimises the complexity of the possible produced water treatment facility.
- In an aspect of the present invention the three phase disc stack centrifuge can be operated at optimal flow rates, according to the following equations:
-
v=flow rate (m3/h) -
gf=the gravitational force of the centrifuge -
r=ratio -
r=g f /v and N1<r<N2 -
Where N1=50 and N2=350 - In one aspect of the present invention the reactant is a sulphide source such as Na2S. Generally it has never been considered to add sulphides to a MEG regeneration and reclamation system due to the risk of formation of toxic H2S. The present inventors have however discovered that in this process, adding a sulphide may provide a selective reaction of heavy metal to precipitate as sulphide, which can be applied to solve the goals of the present invention.
- The present invention will be described in further detail with reference to the enclosed figures with examples of possible embodiments of the invention. Here:
-
FIG. 1 illustrates schematically a first embodiment of the present invention; -
FIG. 2 illustrates schematically a second embodiment of the present invention; -
FIG. 3 illustrates schematically a third embodiment of the present invention; -
FIG. 4 shows a block diagram of an embodiment of the present invention. - The present invention will now be discussed in further detail with reference to the enclosed figures. The figures are schematic illustrations of embodiments of systems and methods according to the present invention. A person skilled in the art will understand that details such as valves, supply of heating and cooling media etc. may have been omitted to better illustrate the main principles of the present invention. In the figures equal reference signs are used to refer to equal elements.
FIG. 1 shows a first embodiment of the present invention. A rich hydrate inhibitor stream 1 comprising hydrate inhibitor, water and a range of dissolved salts enters atank 10 where the rich hydrate inhibitor is brought in contact with astream 2 comprising a selective heavy metal reactant, in a preferred embodiment the reactant is a sulphide source such as Na2S or other sulphide salts and anoptional stream 3 comprising a flocculent. The flocculent is introduced to increase particle size of the precipitate and thereby improving the particle separation. The selectivity of the reactant towards the heavy metal may be influenced by the temperature and the pH of the mixture and optionally coolers or heaters may be installed upstream the on conduit 1. - Optionally the
tank 10 may be equipped with a pH control system with a possibility to regulate the pH close to neutral, pH 5-9, preferably pH=6-8, more preferably pH=6.5-7.5, which gives favourable condition for heavy metal precipitation at the same time avoid precipitation of other divalent cations such as Fe, Ca, Ba, Sr, Mg by having low temperature, below 80° C., preferably below 50° C., more preferably below 30° C. The residence time in thetank 10 is adapted to secure precipitation of the heavy metal. The reacted rich hydrate inhibitor leaves the tank vialine 13 and pump 14, the rich hydrate inhibitor is fed to a three-phasedisk stack centrifuge 20 throughline 15. This three phase separator provides not only separation of the precipitated heavy metal salts from the hydrate inhibitor but also separation of remaining hydrocarbons. The hydrocarbons are removed throughline 21, the heavy metal free rich hydrate inhibitor throughline 19 and the slurry containing the heavy metal particles throughline 23 which feds the slurry to asecond separation system 24 providing solid liquid separation. The liquid phase comprising particle free rich hydrate inhibitor is vialine 29 combined with the main richhydrate inhibitor stream 19. The obtained concentrated heavymetal salt particles 27 will be handled further as hazardous waste. - The combined rich hydrate inhibitor streams now enter what can be considered a traditional pretreatment system consisting of an
initial tank 32 for precipitation of salts of divalent cations. The alkalinity in thetank 32 is controlled by addition of base throughline 31. Examples of applicable bases include: Na2CO3, K2CO3, KOH, NaOH. An appropriate resident time to secure precipitation of the divalent cation salts is obtained through thetank 32. From here the rich hydrate inhibitor is transferred vialine 33, pump 34 andline 35 to asecond centrifuge 36, preferably a disk stack centrifuge. Due to the earlier removal of remaining hydrocarbons thecentrifuge 36 or gravity separator (not shown) will show improved performance.Stream 39 contains the separated divalent cation salts, whereasstream 37 contains partly rich hydrate inhibitor which is being fed to a traditional regeneration andreclamation system 40 providing conventional full stream or slipstream reclamation. The particles instream 39 are non hazardous and neither are the monovalent cation salts that are removed from the hydrate inhibitor during reclamation. -
FIG. 2 illustrates another embodiment of the present invention wherein an embodiment of the particle separation system is described in further detail. Here theslurry stream 23 enters abuffer tank 22 from where it is being fed to a solid-liquid separation unit 26. Solid-liquid separation unit 26 can be but is not limited to filter, basket centrifuge etc. In a start-up situation theunit 26 may not provide acceptable separation and theliquid phase 28 is then return via valve 52 andline 53 to thebuffer tank 22. The quality of the separation is monitored by asensor 50. When the stream quality is increased and thevalve 51 can be opened and the valve 52 closed.Stream 27 will be nearly dry cake of precipitated heavy metal, which can be disposed off safely. - Also illustrated on
FIG. 2 is the optional installation of a second sensor or sampling unit 56 for measuring the efficiency of the heavy metal removal to avoid heavy metals from entering the pretreatment system. -
FIG. 3 illustrates an alternative embodiment of the present invention. Equal units are given equal reference signs. The difference compared toFIGS. 1 and 2 is that the liquid stream from the separation system leaving throughvalve 51 is passed asstream 30 back into theline 15. This system provides the further advantage that in case that heavy metal particles are allowed to pass the filter they will be passed back to the threephase separator 20 and be separated of again. In this embodiment the valve 52 and theline 53 may be obsolete. -
FIG. 4 illustrates an embodiment of the present invention as a block diagram. In this embodiment the hydrate inhibitor is mono ethylene glycol (MEG). A rich MEG feed is fed to a heavy metal precipitation tank to which a precipitant source/reactant e.g. Na2S and flocculent to increase the size and separation of the particles is also fed. The reacted mixture is passed on to a disc stack centrifuge providing separation into three streams, a hydrocarbon/condensate stream, a recovered rich MEG stream and a Heavy metal sludge stream. The heavy metal sludge stream is separated in a solid-liquid separation system providing nearly dry heavy metal precipitate. The solid-liquid separation reduces the rest stream comprising the hazardous mercury to a minimum. The recovered rich MEG enters the pretreatment vessel wherein the alkalinity is controlled to provide for precipitation of salts of divalent cations. The salts are removed in a disk stack centrifuge or a gravity separator providing a divalent cation free rich MEG to regeneration and reclamation and a slurry comprising salts of divalent cations. This slurry will not contain hazardous mercury and therefore need not be treated accordingly.
Claims (17)
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PCT/IB2013/054428 WO2013179236A1 (en) | 2012-05-30 | 2013-05-29 | System and method for removal of heavy metal ions from a rich hydrate inhibitor stream |
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EP (1) | EP2859061B1 (en) |
KR (1) | KR102092029B1 (en) |
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AP (1) | AP3781A (en) |
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WO2018045254A1 (en) * | 2016-09-01 | 2018-03-08 | Schlumberger Technology Corporation | Systems and methods for detection of mercury in hydrocarbon-containing fluids using optical analysis of slug flow |
US10131551B2 (en) * | 2015-06-23 | 2018-11-20 | Conocophillips Company | Separation of kinetic hydrate inhibitors from an aqueous solution |
CN110656902A (en) * | 2019-10-21 | 2020-01-07 | 延安能源化工(集团)有限责任公司 | Drilling fluid waste treatment process and drilling fluid waste treatment device |
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CN104471018A (en) | 2015-03-25 |
BR112014029913B1 (en) | 2021-07-20 |
MY169453A (en) | 2019-04-11 |
KR102092029B1 (en) | 2020-03-24 |
AP3781A (en) | 2016-08-31 |
EP2859061A1 (en) | 2015-04-15 |
KR20150037770A (en) | 2015-04-08 |
EP2859061B1 (en) | 2018-04-11 |
AU2013269181B2 (en) | 2016-03-24 |
CN104471018B (en) | 2017-09-22 |
US9376358B2 (en) | 2016-06-28 |
BR112014029913A2 (en) | 2017-11-21 |
WO2013179236A1 (en) | 2013-12-05 |
AP2014008169A0 (en) | 2014-12-31 |
AU2013269181A1 (en) | 2014-12-18 |
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